Parp Antibody Cell Signaling

In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding.

Parp antibody cell signaling.

Cell s ignaling tec hnology is a t rademark of cell s ignaling tec hnology i nc. Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1. The parp antibody was generated using ppol poly adp ribose polymerase family member 1 parp 1 and parp1 as the antigen. Cell signaling technology s parp antibody is a rabbit polyclonal antibody.

Western blot analysis of extracts from thp 1 cells untreated or treated with tnf α and cycloheximide as well as control extracts from sw620 and a20 cell lines using parp 46d11 rabbit mab. This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5. Various whole cell extracts 30 μg were separated by 5 sds page and the membranes were blotted with parp antibody gtx100573 diluted at 1 2000 and competitor s antibody 9542 diluted at 1 500. 8 7 7 6 1 6 c el l 2 3 5 5 o rd e rs ce l l si g n a l co m su p p o rt.

This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5. The absence of signal in the parp knockout hek293 cells confirms the specificity of the antibody for parp. In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding. Be the first to write a review.

Western blot analysis of extracts from hela cells untreated or treated with staurosporine 9953 1 μm 3 hr jurkat cells untreated or etoposide treated 25 μm overnight and thp 1 cells untreated or cycloheximide treated chx 10 μg ml overnight followed by treatment with tnf α 8902 20 ng ml 4 hr using cleaved parp asp214 d64e10 xp rabbit mab upper or total parp. The hrp conjugated anti rabbit igg antibody gtx213110 01 was used to detect the primary antibody. This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5. Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1.

In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding. This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5. Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1. In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding.

Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1. This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5. In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding. 8 7 7 6 7 8 t ec h 8 3 2 4 w e b.

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